KALAMAZOO, Mich. — Stryker Orthopedics, widely viewed as the largest manufacturer of medical equipment and orthopedic devices, has issued a hazard alert for a specific range of LFIT Anatomic CoCr V40 femoral heads.
Filed Under: Stryker Spine News – Lawsuits, Settlements, Information
In April 2013, Stryker issued an Urgent Medical Device Recall of its OASYS Midline Occipital Plate product line, citing a potentially hazardous defect. According to reports, these devices contain a pin that connects the tulip head to the body of the plate, and this pin was fracturing post-operatively in some patients. Fracture of this pin […]
Stryker spine plate lawsuits are being filed throughout the United States due to serious complications that have surfaced. These spinal plates are small medical devices that are used in spinal fusion procedures; they work to help stabilize the area where the occipital bone and vertebrae meet in the cervical spine. Unfortunately, Strykers spine plates have […]
Stryker’s OASYS spine plate product line are medical devices that are used in cervical spinal fusion procedures. The spine plates are meant to be permanently implanted into the spine of patients. These devices hit the market in April 2010 and have been used for patients who require stabilization where the occipital bone and the vertebrae […]
KALAMAZOO, Mich. — Orthopedic giant Stryker is hoping a new medical device will ease the pain from its disastrous release of the OASYS Midline Occipital Plate.